Mangani-pargasite, NaCa2(Mg4Mn3+)(Si6Al2)O22(OH)2, a new mineral species of the amphibole supergroup

Mangani-pargasite, ideally NaCa2(Mg4Mn3+)(Si6Al2)O22(OH)2, is a new mineral species of the calcium amphibole subgroup of the amphibole supergroup. The type specimen was found on the mine dump of the Långban Fe-Mn-(Ba-As-Pb-Sb) deposit in Värmland, Sweden. Crystal chemical analyses resulted in the empirical chemical formula: A(Na0.90Pb0.07K0.03)Σ1.00B(Ca1.93Mn2+0.07)Σ2.00C(Mg4.25Mn3+0.39Al0.26 Fe3+0.10)Σ5.00T(Si6.35Al1.65)Σ8.00O22W(OH)2. In order to complete the description of this newly approved (IMA 2018-151) mineral we report here additional data to those published in papers by Jonsson and Hålenius (2010) and Hålenius and Bosi (2012). Mangani-pargasite is biaxial positive, with a=1.635(5), b=1.645(5), g=1.660(5) and the measured optic angle 2V is 85(5)°. The dispersion is weak (r>v), and the optic orientation is: Y||b; Z^c=25(3)°. Mangani-pargasite is red to brownish red with weak pleochroism; X=pale reddish brown, Y=pale reddish brown and Z=pale brownish red; X≈Y>Z. The unit-cell parameters are a=9.9448(5), b=18.0171(9), c=5.2829(3) Å, b=105.445(3)°, V=912.39(9) Å3, Z=2, space group C2/m. The ten strongest reflections in the X-ray powder diffraction pattern [d-values in Å, I, (h k l)] are: 8.420, 29, (110); 3.368, 17, (131), 3.279, 49, (240); 3.141, 100, (310); 2.817, 44, (33 0); 2.698, 21, (151); 2.389, 18, (350); 1.904, 29, (510); 1.650, 22, (461) and 1.448, 46, (661)

Heliophyllite: A discredited mineral species identical to ecdemite

The type material for heliophyllite, preserved in the Swedish Museum of Natural History in Stockholm, was re-investigated through a combined EPMA (electron probe X-ray microanalysis), Raman, and X-ray powder diffraction (XRPD) and single-crystal study. EPMA chemical data, together with Raman and single-crystal structural studies, point to heliophyllite being identical to ecdemite. XRPD synchrotron data highlight the presence of a minor quantity of finely admixed finnemanite in the analyzed material, explaining the presence of some additional diffraction peaks, not indexable with the ecdemite unit cell, reported in the literature. The discreditation of heliophyllite has been approved by the IMA Commission on New Minerals and Mineral Names (proposal 19-H, 2019)

Crystal chemistry of sulfates from the apuan alps (Tuscany, Italy). V. Scordariite, K8(Fe3+0.67 0.33)[Fe3+3O(SO4)6(H2O)3]2(H2O)11: A new metavoltine-related mineral

The new mineral species scordariite, K8(Fe3+0.67 0.33)[Fe3+3O(SO4)6(H2O)3]2(H2O)11, was discovered in the Monte Arsiccio mine, Apuan Alps, Tuscany, Italy. It occurs as pseudo-hexagonal tabular crystals, yellowish to brownish in color, up to 0.5 mm in size. Cleavage is perfect on 0001. It is associated with giacovazzoite, krausite, gypsum, jarosite, alum-(K), and magnanelliite. Electron microprobe analyses give (wt %): SO3 47.31, Al2O3 0.66, Fe2O3 24.68, FeO 0.69, Na2O 0.52, K2O 17.36, H2Ocalc 15.06, total 106.28. The partitioning of Fe between Fe2+ and Fe3+ was based on Mössbauer spectroscopy. On the basis of 67 O atoms per formula unit, the empirical chemical formula is (K7.50Na0.34)Σ7.84(Fe3+6.29Al0.26Fe2+0.20)Σ6.75S12.02O50·17H2O. The ideal end-member formula can be written as K8(Fe3+0.67 0.33)[Fe3+3O(SO4)6(H2O)3]2(H2O)11. Scordariite is trigonal, space group R-3, with (hexagonal setting) a = 9.7583(12), c = 53.687(7) Å, V = 4427.4(12) Å3, Z = 3. The main diffraction lines of the observed X-ray powder pattern are [d(in Å), estimated visual intensity]: 8.3, strong; 6.6, medium; 3.777, medium; 3.299, medium; 3.189, medium; 2.884, strong. The crystal structure of scordariite has been refined using X-ray single-crystal data to a final R1 = 0.057 on the basis of 1980 reflections with Fo > 4σ(Fo) and 165 refined parameters. It can be described as a layered structure formed by three kinds of layers. As with other metavoltine-related minerals, scordariite is characterized by the occurrence of the [Fe3+3O(SO4)6(H2O)3]5- heteropolyhedral cluster

Nickel-and Fe3+-rich oxy-dravite from the Artana Mn prospect, Apuan Alps (Tuscany, Italy)

Nickel-and Fe3+-rich oxy-dravite was identified on a specimen collected in the Artana Mn prospect, Carrara, Apuan Alps, Tuscany, Italy. Oxy-dravite occurs as brownish-orange prismatic crystals, up to 0.3 mm in length, associated with quartz, carbonates, and hematite. Electron microprobe analysis gave (in wt. % – average of 7 spot analyses): SiO2 35.81, TiO2 0.41, B2 O3(calc) 10.38, Al2 O3 29.36, V2 O3 0.78, Cr2 O3 0.09, Fe2 O3 3.32, FeO 0.33, MgO 8.04, CaO 0.39, MnO 0.34, NiO 3.46, ZnO 0.40, Na2 O 2.84, F 0.29, H2 O(calc) 3.00, O = F –0.12, total 99.12. The Fe3+/Fetot ratio was calculated based on optical absorption spectroscopy. The empirical ordered formula of the studied sample is (with rounding errors)X(Na0.92 Ca0.07 □0.01)Σ1.00 Y (Mg2.01 Ni2+0.47Fe3+ Ti0.33 0.05Mn2+0.05Fe2+ Zn)Z (Al 0.05 0.05 Σ3.005.80 V0.10 Cr0.01 Fe3+) Si O (BO)V (OH) 0.09 Σ6.00 6 18 3 33W [O0.50 (OH)0.35 F0.15 ]Σ1.00 . This is an intermediate member of the dravite–oxy-dravite series. In naming it, the prefix oxy-was preferred sinceWO is very close to being larger than 0.5 atoms per formula unit. Infrared spectroscopy revealed the occurrence of significant amounts ofW(OH), and allowed to propose a specific short-range arrangements around the O(1) and O(3) sites. Unit-cell parameters are a = 15.9349(11), c = 7.2038(5) Å, V = 1584.1(2) Å3, space group R3m. The crystal structure was refined by single-crystal X-ray diffraction data to R1 = 0.0146 on the basis of 1138 unique reflections with Fo > 4σ(Fo) and 94 refined parameters. The optimized crystal-chemical formula isX(Na0.92 Ca0.07 □0.01)Σ1.00Y (Mg1.21 Al0.80 Ni2+0.47Fe3+0.26 Ti0.05 Mn2+ Zn V Cr)Z (Al 0.05 0.05 0.10 0.01 Σ3.005.00 Mg0.80 Fe3+ 0.16Fe2+) Si O (BO) O(3) O(1) (OH) 0.05 Σ6.00 6 18 3 33 [O0.50 (OH)0.35 F0.15 ]Σ1.00 . Nickel is ordered at the Y site, in agreement with results obtained on synthetic tourmalines. Oxy-dravite is likely the result of the metamorphic recrystallization of Mn-rich layers at the top of the Liassic carbonates belonging to the Marble Formation of the Apuan Alps Metamorphic Complex

Сетевая система контроля технологического процесса выращивания полупроводниковых кристаллов и тонких пленок

Экспериментальное моделирование аппаратно-программного обеспечения показало достаточную надежность работы системы и значительное уменьшение трудоемкости контроля и управления параметрами технологического процесса

Brattforsite, Mn19(AsO3)12Cl2, a new arsenite mineral related to magnussonite, from Brattforsgruvan, Nordmark, Värmland, Sweden

Brattforsite is an approved mineral (IMA2019-127), with ideal formula Mn19(AsO3)12Cl2. Associated minerals in the type specimen from the Brattfors mine, Nordmark (Värmland, Sweden) include jacobsite, alleghanyite, phlogopite, calcite and dolomite. Brattforsite, forming subhedral, mostly equant crystals up to 0.5 mm across, is orange to reddish-brown with a white streak, and translucent with a resinous to vitreous lustre. The fracture is uneven to subconchoidal, and no cleavage is observed. It is very weakly pleochroic in yellow, optically biaxial (–) with 2V = 44(5)° and has calculated mean refractive index of 1.981. Measured and calculated density values are 4.49(1) and 4.54(1) g·cm− 3, respectively. Chemical analyses yields (in wt%): MgO 0.62, CaO 1.26, MnO 48.66, FeO 0.13, As2O3 46.72, Cl 2.61, H2Ocalc 0.07, O ≡ Cl –0.59, sum 99.49, corresponding to the empirical formula (Mn17.67Ca0.58Mg0.40Fe0.05)∑18.70As12.17O35.90Cl1.90(OH)0.20, based on 38 (O + Cl + OH) atoms per formula unit. The five strongest Bragg peaks in the powder X-ray diffraction pattern are [d (Å), I (%), (hkl)]: 2.843,100, (4 - 44); 2.828, 99, (444); 1.731, 32, (880); 2.448, 28, (800); 1.739, 25, (088). Brattforsite is monoclinic and pseudotetragonal, space group I2/a, with unit-cell parameters a = 19.5806(7), b = 19.5763(7), c = 19.7595(7) Å, β = 90.393(3)°, V = 7573.9(5) Å3 and Z = 8. The crystal structure was solved and refined to an R1 index of 3.4 % for 7445 reflections [Fo > 4σ(Fo)]. Brattforsite has the same overall structural topology as magnussonite (i.e., the species can be considered as homeotypic), but with 12 independent tetrahedrally coordinated As sites and 21 Mn sites with varying (4–8) coordination. The Mn-centered polyhedra, bonded through edge- and face-sharing, give rise to a three-dimensional framework. The (AsO3)3− groups are bonded to this framework through corner- and edge-sharing. Spectroscopic measurements (optical absorption, Raman, FTIR) carried out support the interpretation of the compositional and structural data

Thermally induced cation redistribution in fluor-elbaite and Fe-bearing tourmalines

An Fe-rich fluor-elbaite was thermally treated in air and hydrogen atmosphere up to 800 °C to study potential changes in Fe- and Al-ordering over the octahedrally coordinated Y and Z sites. Overall, the experimental data (structural refinement, electron and ion microprobe, Mössbauer, infrared and optical absorption spectroscopy) show that thermal treatment of fluor-elbaite results in an increase of Fe contents at the Z site balanced by an increase of Al at the Y site. On the basis of this and previous experimental studies on Fe–Mg–Al-bearing tourmalines, it can be stated that the intersite Fe–Mg–Al exchange rates are significant at temperatures around 700–800 °C. Thermal treatment results in an increase of ca. 0.30 Fe atoms per formula unit at the Z site compensated by a similar increase of (Mg + Al) at the Y site, following the exchange reaction Y Fe + Z (Mg + Al) → Z Fe + Y (Mg + Al). Since the tourmaline nomenclature is based on the occupancy of ions at each structural site, the intersite Fe–Mg–Al ordering may determine the tourmaline species. This means that effectively the name associated with a given composition may be a function of the sample thermal history